HADH antibody
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935106861
info@markelab.com
name
HADH antibody
category
Primary Antibodies
provider
FineTest
reference
FNab03747
tested applications
ELISA, WB, IHC
Description
This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | hydroxyacyl-Coenzyme A dehydrogenase (HADH) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 33 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | Q16836 |
| Gene ID | 3033 |
| Alias | Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial (HCDH),Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase,Short-chain 3-hydroxyacyl-CoA dehydrogenase,HADH,HAD,HAD1,HADHSC,SCHAD |
| Background | Antibody anti-HADH |
| Status | RUO |
| Note | Mol. Weight 33 kDa |
Descripción
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Human HADH (Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial) ELISA Kit
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HADH antibody
This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.
Ver Producto